This is a fantastic opportunity for a Manufacturing Associate to join a world-class team. You'll be working at a state-of-the-art manufacturing facility that specializes in developing life-saving treatments, where you'll contribute to the production of essential drug substances. This role offers an engaging, hands-on experience in a cGMP commercial environment with a company dedicated to producing high-quality biopharmaceuticals.
You'll have the chance to apply your skills in downstream manufacturing and will spend a significant portion of your day working in a gowned, aseptic environment. With a primary focus on documentation, quality control, and the daily operations of a pharmaceutical production line, this role is a great fit for someone who is detail-oriented and thrives in a structured, fast-paced setting.
location: Pearl River, New York
job type: Contract
salary: $25.00 - 26.60 per hour
work hours: 9 to 5
education: High School
responsibilities:
- Operate and maintain a variety of downstream processing equipment, including centrifuges, filtration systems, and chromatography columns.
- Ensure accurate documentation of batch records and adherence to good documentation practices (GDP).
- Prepare equipment for manufacturing by performing cleaning and sanitization procedures (CIP/SIP).
- Follow established Standard Operating Procedures (SOPs) for materials, personnel, and equipment flow within the facility.
- Manage and analyze manufacturing data while also identifying and troubleshooting issues.
- Perform routine equipment preparation, including the weighing and dispensing of raw materials.
- Collaborate with other departments to resolve any quality issues that may arise during manufacturing.
qualifications:
Required:
- High School degree with at least two years of work experience, or relevant training in a cGMP manufacturing environment.
- At least one year of experience in GMP/Pharma manufacturing.
- Proficiency in English, both written and spoken.
- Strong communication and social skills.
- Good documentation skills and attention to detail.
- General knowledge of cGMP, GDP, and SOPs.
- Basic understanding of the Baculovirus Expression Vector System (BEVS) manufacturing process.
skills: SOP, Good Manufacturing Practices (GMP), Corrective and Preventive Actions (CAPA), Good Documentation Practices (GDP)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
